Tonelli Marcello, Hemmelgarn Brenda, Reiman Tony, Manns Braden, Reaume M Neil, Lloyd Anita, Wiebe Natasha, Klarenbach Scott
Department of Medicine, University of Alberta, Edmonton.
CMAJ. 2009 May 26;180(11):E62-71. doi: 10.1503/cmaj.090470. Epub 2009 Apr 30.
BACKGROUND: Erythropoiesis-stimulating agents are used to treat anemia in patients with cancer. However, their safety and effectiveness is controversial. We did a systematic review of the clinical efficacy and harms of these agents in adults with anemia related to cancer or chemotherapy. METHODS: We conducted a systematic review of published and unpublished randomized controlled trials (RCTs) using accepted methods for literature searches, article selection, data extraction and quality assessment. We included RCTs involving anemic adults with cancer. We compared the use of erythropoiesis-stimulating agents with nonuse and assessed clinical outcomes (all-cause mortality, cardiovascular events and hypertension, health-related quality of life, blood transfusions and tumour response) and harms (serious adverse events) between groups. RESULTS: We identified 52 trials (n = 12 006) that met our selection criteria. The pooled all-cause mortality during treatment was significantly higher in the group receiving erythropoiesis-stimulating therapy than in the control group (relative risk [RR] 1.15, 95% confidence interval [CI] 1.03 to 1.29). Compared with no treatment, use of erythropoiesis-stimulating agents led to clinically detectable improvements in disease-specific measures of quality of life. It also reduced the use of blood transfusions (RR 0.64, 95% CI 0.56 to 0.73). However, it led to an increased risk of thrombotic events (RR 1.69, 95% CI 1.27 to 2.24) and serious adverse events (RR 1.16, 95% CI 1.08 to 1.25). INTERPRETATION: Use of erythropoiesis-stimulating agents in patients with cancer-related anemia improved some disease-specific measures of quality of life and decreased the use of blood transfusions. However, it increased the risk of death and serious adverse events. Our findings suggest that such therapy not be used routinely as an alternative to blood transfusion in patients with anemia related to cancer.
背景:促红细胞生成素用于治疗癌症患者的贫血。然而,其安全性和有效性存在争议。我们对这些药物在与癌症或化疗相关的成人贫血患者中的临床疗效和危害进行了系统评价。 方法:我们采用公认的文献检索、文章筛选、数据提取和质量评估方法,对已发表和未发表的随机对照试验(RCT)进行了系统评价。我们纳入了涉及癌症贫血成人的RCT。我们比较了促红细胞生成素的使用与不使用情况,并评估了两组之间的临床结局(全因死亡率、心血管事件和高血压、健康相关生活质量、输血和肿瘤反应)和危害(严重不良事件)。 结果:我们确定了52项符合我们纳入标准的试验(n = 12006)。接受促红细胞生成素刺激治疗组在治疗期间的合并全因死亡率显著高于对照组(相对风险[RR] 1.15,95%置信区间[CI] 1.03至1.29)。与未治疗相比,使用促红细胞生成素可使生活质量的疾病特异性指标在临床上得到可检测到的改善。它还减少了输血的使用(RR 0.64,95% CI 0.56至0.73)。然而,它导致血栓形成事件的风险增加(RR 1.69,95% CI 1.27至2.24)和严重不良事件的风险增加(RR 1.16,95% CI 1.08至1.25)。 解读:在癌症相关贫血患者中使用促红细胞生成素可改善一些生活质量的疾病特异性指标,并减少输血的使用。然而,它增加了死亡风险和严重不良事件的风险。我们的研究结果表明,在癌症相关贫血患者中,这种治疗不应常规用作输血的替代方法。
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